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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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2531 Rip resistant — 1 UDI-DI variant, MDR (4Care Nederland B.V.)

MD Atlas
4Care Nederland B.V.

Data from EUDAMED, last updated May 31, 2026

2531 Rip resistant

40517082531KB

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: 4Care Nederland B.V.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40517082531KB
Device name: 2531 Rip resistant
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 12, 2025

Manufacturer & authorised representative

Manufacturer

Name: 4Care Nederland B.V.
SRN: NL-MF-000050317
Country: Netherlands
Email: info@4care.eu
Phone: +31497643236

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01K9W5TSQN2YJJF4W4K42W0BAW

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Rip-resistant bodysuit 253104051708008719